Novel familial <i>KDF1</i> mutation detected in members of a three-generation family with clinical manifestations of ectodermal dysplasia: A report of four cases. [PDF]
Keramida C +11 more
europepmc +1 more source
Novel homozygous frameshift insertion variant in the last exon of the EDARADD causing hypohidrotic ectodermal dysplasia in two siblings: case report and review of the literature. [PDF]
Kablan A, Tasdelen E.
europepmc +1 more source
Attitudes of female carriers of X-linked hypohidrotic ectodermal dysplasia towards prenatal treatment and their decisions during a pregnancy with a male fetus. [PDF]
Schneider H +10 more
europepmc +1 more source
Ectodermal dysplasia: a narrative review of the clinical and biological aspects relevant to oral health. [PDF]
Morandini AC +11 more
europepmc +1 more source
Dental Implants as a Treatment Option for Prosthetic Rehabilitation of Children with Ectodermal Dysplasia: A Systematic Review. [PDF]
Barve KD, Padawe DS, Takate VS.
europepmc +1 more source
Ektodüsplasiini ekspressioon punakõrv-ilukilpkonna Trachemys scripta arengus [PDF]
Rebane, Anni
core
Genodermatosis among the southwestern Saudi population: The pattern and the need for a premarital genetic screening protocol. [PDF]
Alfahaad HA.
europepmc +1 more source
Prenatal genetic testing and potential consequences. [PDF]
Jauch SF, Klaritsch P.
europepmc +1 more source
Ectodermal organ development : Regulation by Notch and Eda pathways [PDF]
Mustonen, Tuija
core
[Hypohidrotic ectodermal dysplasia].
S, Campuzano Martín +3 more
openaire +1 more source

